Calcium-binding photoprotein

ABSTRACT

The invention provides calcium-binding photoproteins which can detect light emission with a higher sensitivity. The proteins of the invention comprising the amino acid sequence of SEQ ID NO: 2 can be used for the detection and measurement of calcium ions. The proteins of the invention are useful as reporter proteins, luminescent markers, etc. The polynucleotides of the invention are useful as reporter genes, etc.

TECHNICAL FIELD

The present invention relates to calcium-binding photoproteins, genesencoding the same and use thereof.

BACKGROUND OF THE INVENTION

The calcium-binding photoproteins are present as a complex of anapoprotein and the peroxide of coelenterazine as a light-emittingsubstrate. The calcium-binding photoproteins emit a flash of light whenbound to calcium ions.

Among the calcium-binding photoproteins including aequorin, obelin,clytin, mitrocomin, mineopsin and bervoin, aequorin is awell-characterized calcium-binding photoprotein, and its proteinstructure and the luminescence mechanism have been reported in detail(see, e.g., Inouye et al. (1985) Proc. Natl. Acad. Sci. USA 82,3154-3158; and Head et al. (2000) Nature 405, 372-376). Due to its highsensitivity to calcium ions, aequorin is used to detect/quantify traceamounts of calcium ions, to measure changes in the concentration ofintracellular calcium ions, and so on.

Clytin is a calcium-binding photoprotein isolated from the luminousjellyfish Clytia gregoria (see Inouye, S, and Tsuji, F. I. (1993) FEBSLett, 315, 343-346; etc.). Clytin is present as a complex of apoclytinand the peroxide of coelenterazine as the light-emitting substrate. Whenbound to calcium ions, clytin emits a flash of light to producecoelenteramide, which is the oxidation product of coelenterazine, andcarbon dioxide.

Herein, clytin can be classified into two groups, clytin-I and clytin-II(see, e.g., JPA 2008-22848; and Inouye, S (2008) J. Biochem. 143,711-717). Of these two groups, clytin-H emits a flash of light whenbound to calcium ions. The decay time of luminescence in clytin-II is ashorter than that of clytin-I.

DISCLOSURE OF INVENTION

Under the foregoing circumstances, there have been desiredcalcium-binding photoproteins which show a rapid decay pattern ofluminescence and have a detectable luminescence with high sensitivity.

In order to solve the foregoing problems, the present inventors havemade extensive investigations and as a result, have found that proteinscomprising the amino acid sequence of SEQ ID NO: 2, etc. have thefunction capable of binding to the peroxide of coelenterazine or theperoxide of coelenterazine derivatives to form holoproteins that emitlight by calcium ions. The inventors have also found that when theholoproteins described above are bound to calcium ions, a rapid decaypattern of luminescence is shown and the luminescence can be detectedwith a high sensitivity. Based on these findings, further investigationshave been made and the present invention has come to be accomplished.

The present invention provides the following proteins, polynucleotides,recombinant vectors, transformants, and so on.

(1) A protein as defined by any one of (a) through (d) below:

-   (a) a protein consisting of the amino acid sequence of SEQ ID NO. 2;-   (b) a protein consisting of the amino acid sequence of SEQ ID NO. 2,    wherein the amino acids at positions 107, 110, 120, 140, 179 and 180    are aspartic acid, aspartic acid, glycine, proline, threonine and    serine, respectively, and one to several amino acid(s) except for    the amino acid(s) at the positions above are substituted with other    amino acid(s), and having the binding ability to the peroxide of    coelenterazine or the peroxide of a coelenterazine derivative to    form a holoprotein that emits light by calcium ions;-   (c) a protein comprising the amino acid sequence of SEQ ID NO: 2,    and having the binding ability to the peroxide of coelenterazine or    the peroxide of a coelenterazine derivative to form a holoprotein    that emits light by calcium ions; and,-   (d) a protein comprising the amino acid sequence of SEQ ID NO. 2,    wherein the amino acids at positions 107, 110, 120, 140, 179 and 180    are aspartic acid; aspartic acid, glycine, proline, threonine and    serine, respectively, and one to several amino acid(s) except for    the amino acid(s) at the positions above are substituted with other    amino acid(s), and having the binding ability to the peroxide of    coelenterazine or the peroxide of a coelenterazine derivative to    form a holoprotein that emits light by calcium ions.

(2) The protein according to (1) above, which is any one of (a) through(d) below:

-   (a) a protein consisting of the amino acid sequence of SEQ ID NO. 2;-   (b) a protein consisting of the amino acid sequence of SEQ ID NO. 2,    wherein the amino acids at positions 107, 110, 120, 140, 179 and 180    are aspartic acid, aspartic acid, glycine, proline, threonine and    serine, respectively, and 1 to 16 amino acid(s) except for the amino    acid(s) at the positions above are substituted with other amino    acid(s), and having the binding ability to the peroxide of    coelenterazine or the peroxide of a coelenterazine derivative to    form a holoprotein that emits light by calcium ions;-   (c) a protein comprising the amino acid sequence of SEQ ID NO: 2,    and having the binding ability to the peroxide of coelenterazine or    the peroxide of a coelenterazine derivative to form a holoprotein    that emits light by calcium ions; and,-   (d) a protein comprising the amino acid sequence of SEQ ID NO. 2,    wherein the amino acids at positions 107, 110, 120, 140, 179 and 180    are aspartic acid, aspartic acid, glycine, proline, threonine and    serine, respectively, and 1 to 16 amino acid(s) except for the amino    acid(s) at the positions above are substituted with other amino    acid(s), and having the binding ability to the peroxide of    coelenterazine or the peroxide of a coelenterazine derivative to    form a holoprotein that emits light by calcium ions.

(3) The protein according to (1) above, which is any one of (a) through(d) below:

-   (a) a protein consisting of the amino acid sequence of SEQ ID NO. 2;-   (b) a protein consisting of the amino acid sequence of SEQ ID NO. 2,    wherein the amino acids at positions 107, 110, 120, 140, 179 and 180    are aspartic acid, aspartic acid, glycine, proline, threonine and    serine, respectively, and 1 to 6 amino acid(s) except for the amino    acid(s) at the positions above are substituted with other amino    acid(s), and having the binding ability to the peroxide of    coelenterazine or the peroxide of a coelenterazine derivative to    form a holoprotein that emits light by calcium ions;-   (c) a protein comprising the amino acid sequence of SEQ ID NO: 2,    and having the binding ability to the peroxide of coelenterazine or    the peroxide of a coelenterazine derivative to form a holoprotein    that emits light by calcium ions; and,-   (d) a protein comprising the amino acid sequence of SEQ ID NO. 2,    wherein the amino acids at positions 107, 110, 120, 140, 179 and 180    are aspartic acid, aspartic acid, glycine, proline, threonine and    serine, respectively, and 1 to 6 amino acid(s) except for the amino    acid(s) at the positions above are substituted with other amino    acid(s), and having the binding ability to the peroxide of    coelenterazine or the peroxide of a coelenterazine derivative to    form a holoprotein that emits light by calcium ions.

(4) The protein according to (1) above which is (a) or (b) below

-   (a) a protein consisting of the amino acid sequence of SEQ ID NO. 2;    or,-   (b) a protein comprising the amino acid sequence of SEQ ID NO: 2,    and having the binding ability to the peroxide of coelenterazine or    the peroxide of a coelenterazine derivative to form a holoprotein    that emits light by calcium ions.

(5) The protein according to any one of (1) through (4) above, furthercomprising a peptide sequence and/or secretory signal peptide forpurification.

(6) A holoprotein comprising the protein according to any one of (1)through (5) above and the peroxide of coelenterazine or the peroxide ofa coelenterazine derivative.

(7) A polynucleotide comprising a polynucleotide encoding the proteinaccording to any one of (1) through (5) above

(8) A recombinant vector comprising the polynucleotide according to (7)above.

(9) A transformant having inserted therein the recombinant vectoraccording to (8) above.

(10) A method of producing the protein according to any one of (1)through (5) above, which comprises culturing the transformant of (9)above to produce the protein according to any one of (1) through (5)above.

(11) A kit comprising the protein according to any one of (1) through(5) above or the holoprotein according to (6) above.

(12) A kit comprising the polynucleotide of (7) above, the recombinantvector of (8) above or the transformant of (9) above.

(13) A method of detecting or quantifying a calcium ion, which comprisesusing the protein according to any one of (1) to (5) above or theholoprotein according to (6) above.

(14) A method of assaying the activity of a sequence associated withpromoter control, which comprises using the polynucleotide of (7) aboveas a reporter gene.

(15) A method of measuring changes in intracellular calciumconcentration, which comprises the step of expressing the polynucleotideof (7) above in a cell to form a photoprotein.

(16) A method of producing a fluorescent protein, which comprisesreacting the protein according to any one of (1) through (5) above withcoelenteramide or an analogue thereof in the presence or absence of acalcium ion or a divalent or trivalent ion that can be substituted forthe calcium ion.

(17) The method according to (16) above, wherein the reaction is carriedout in the presence of a reducing agent

(18) The method according to (16) or (17) above, wherein the reaction iscarried out in the presence of a chelating agent to remove the calciumion or the divalent or trivalent ion that can be substituted for thecalcium ion.

The protein of the present invention can bind to the peroxide ofcoelenterazine or the peroxide of coelenterazine derivatives to form aholoprotein that emits light by calcium ions. The holoprotein producedfrom the protein in some embodiments of the invention provides a rapiddecay pattern of luminescence and the luminescence can be detected withhigh sensitivity.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 shows the construction of the expression vector pBlue-CLI-ESNA(EXAMPLE 1), wherein (A) shows a schematic representation ofpBlue-CLI-ESNA and (B) shows a schematic representation of thenucleotide sequence of pBlue-CLI-ESNA.

FIG. 2 shows the construction of the expression vector piP-H-CLI-ESNA(EXAMPLE 3), wherein (A) shows a schematic representation ofpiP-H-CLI-ESNA and (B) shows a schematic representation of thenucleotide sequence of piP-H-CLI-ESNA.

FIG. 3 shows the results of SDS-PAGE analysis (EXAMPLE 4). Lane 1:Protein molecular weight markers (Tefco), Lane 2: Supernatant(corresponding to 100 μl of the cultured bacterial cells) obtained bycentrifugation at 5,000 g for 10 minutes from the ultrasonicated lysateof transformants expressing piP-H-CLI-ESNA in E. coli; Lane 3: Fractioneluted from a nickel-chelate column (protein level, 29.5 μg); Lane 4:Fraction eluted from a butyl sepharose column (protein level, 2.2 μg).

FIG. 4 shows the measurement results of luminescence patterns forCLA-ESNA, AQ (aequorin), CL-I (clytin-II) and Ob (obelin) (EXAMPLE 6).

FIG. 5 shows the bioluminescence spectrum of recombinant clytin-ESNA andthe fluorescence spectrum of the synthetic fluorescent proteins preparedfrom recombinant apoclytin-ESNA and coelenteramide.

-   A: Bioluminescence emission spectrum of recombinant clytin-ESNA by    the addition of a calcium solution-   B: Fluorescence spectrum of the calcium-binding synthetic    fluorescent protein prepared from recombinant apoclytin-ESNA and    coelenteramide by excitation light at 335 nm-   C: Fluorescence spectrum of the calcium-free synthetic fluorescent    protein prepared from recombinant apoclytin-ESNA and coelenteramide    by excitation light at 335 nm

BEST MODES FOR CARRYING OUT THE INVENTION

Hereinafter the present invention is described in detail with referenceto the embodiments,

1. Protein of the Invention

The protein of the invention refers to a protein consisting of the aminoacid sequence of SEQ ID NO: 2 and a protein which has substantially thesame activity or function as the protein consisting of the amino acidsequence of SEQ ID NO: 2.

The term substantially the same activity or function is used to mean,for example, (i) the function that the protein above is capable ofbinding to the peroxide of coelenterazine or the peroxide ofcoelenterazine derivatives to form holoproteins, (ii) the function thatthe protein above is capable of binding to the peroxide ofcoelenterazine or the peroxide of coelenterazine derivatives to formholoproteins that emit light by calcium ions; (iii) a maximum intensity(Imax) of the luminescence generated by binding of the holoproteindescribed above to calcium ions is approximately ¼ or more, preferablyapproximately ⅓ or more, more preferably approximately ½ or more, andmost preferably approximately 1/1.5, the maximum luminescence intensity(Imax) of the protein consisting of the amino acid sequence of SEQ IDNO: 2; and (iv) a half-life period (T_(1/2), in seconds) of theluminescence generated by binding the holoproteins described above tocalcium ions is 4 times or less, preferably approximately 3 times orless, more preferably approximately 2 times or less, and most preferablyapproximately 1.5 times or less, the half-life (T_(1/2), in seconds) ofthe protein consisting of the amino acid sequence of SEQ ID NO: 2. Theluminescence activity and luminescence pattern above may be determinedby the methods described in, for example, Shimomura, O. et al., Biochem.J., 251, 405-410 (1988); Shimomura, O. et al., Biochem. J., 261, 913-920(1989); etc.

Specifically, a luminescence reaction is initiated by adding a calciumsolution to the holoprotein above, and the luminescence activity orpattern can be measured using a luminometer. Luminometers which may beused include commercially available instruments such as TD-4000(manufactured by Labo Science) and Centro LB 960 (manufactured byBerthold).

As used herein, the term “a protein binds to the peroxide ofcoelenterazine or the peroxide of a coelenterazine derivative to form aholoprotein” means not only (1) that a protein binds to the peroxide ofcoelenterazine or the peroxide of a coelenterazine derivative to form aholoprotein but also (2) that a protein is brought in contact with theperoxide of coelenterazine or the peroxide of its derivative in thepresence of oxygen to form a holoprotein (complex) containing theprotein and the peroxide of coelenterazine or the peroxide of acoelenterazine derivative.

As used herein, the term coelenterazine derivative refers to a compoundthat binds to the protein of the invention to form a holoprotein capableof emitting light by calcium ions.

More specifically, the protein of the present invention includes, forexample:

(a) a protein consisting of the amino acid sequence of SEQ ID NO. 2;

(b) a protein consisting of the amino acid sequence of SEQ ID NO. 2,wherein the amino acids at positions 107, 110, 120, 140, 179 and 180 areaspartic acid, aspartic acid, glycine, proline, threonine and serine,respectively, and one to several amino acid(s) except for the aminoacid(s) at the positions above are substituted with other amino acid(s),and having substantially the same activity or function as the proteinconsisting of the amino acid sequence of SEQ ID NO. 2;

(c) a protein comprising the amino acid sequence of SEQ ID NO: 2 andhaving substantially the same activity or function as the proteinconsisting of the amino acid sequence of SEQ ID NO. 2;

(d) a protein comprising the amino acid sequence of SEQ ID NO. 2,wherein the amino acids at positions 107, 110, 120, 140, 179 and 180 areaspartic acid, aspartic acid, glycine, proline, threonine and serine,respectively, and one to several amino acid(s) except for the aminoacid(s) at the positions above are substituted with other amino acid(s),and having substantially the same activity or function as the proteinconsisting of the amino acid sequence of SEQ ID NO: 2; and the like.

The protein comprising the amino acid sequence of SEQ ID NO: 2 includes,for example,

(a) a protein consisting of the amino acid sequence of SEQ ID NO: 2, 4or 6;

(b) a protein comprising the amino acid sequence of SEQ ID NO: 2, 4 or6; and the like.

The protein comprising the amino acid sequence of SEQ ID NO. 2, whereinthe amino acids at positions 107, 110, 120, 140, 179 and 180 areaspartic acid, aspartic acid, glycine, praline, threonine and serine,respectively, and one to several amino acid(s) except for the aminoacid(s) at the positions above are substituted with other amino acid(s)includes:

(a) a protein consisting of the amino acid sequence of SEQ ID NO. 2,wherein the amino acids at positions 107, 110, 120, 140, 179 and 180 areaspartic acid, aspartic acid, glycine, proline, threonine and serine,respectively, and one to several amino acid(s) except for the aminoacid(s) at the positions above are substituted with other amino acid(s);

(b) a protein comprising the amino acid sequence of SEQ ID NO. 2,wherein the amino acids at positions 107, 110, 120, 140, 179 and 180 areaspartic acid, aspartic acid, glycine, praline, threonine and serine,respectively, and one to several amino acid(s) except for the aminoacid(s) at the positions above are substituted with other amino acid(s);and the like.

The term “one to several amino acid(s) are substituted” described aboveis used to mean that one or more amino acid residues are substituted atany one or more positions in the same amino acid sequence.

Hereinafter, examples of mutually substitutable amino acid residues areen are given below. Amino acid residues in the same group can bemutually substituted.

-   Group A: leucine, isoleucine, norleucine, valine, norvaline,    alanine, 2-aminobutanoic acid, methionine, o-methylserine,    t-butylglycine, t-butylalanine and cyclohexylalanine;-   Group B: aspartic acid, glutamic acid, isoaspartic acid, isoglutamic    acid, 2-aminoadipic acid and 2-aminosuberic acid;-   Group C: asparagine and glutamine;-   Group D: lysine, arginine, ornithine, 2,4-diaminobutanoic acid and    2,3-diaminopropionic acid;-   Group E: proline, 3-hydroxyproline and 4-hydroxyproline;-   Group F: serine, threonine and homoserine, and,-   Group G: phenylalanine and tyrosine.

As used herein, the range of “one to several” in “the amino acidsequence in which one to several amino acid(s) are substituted withother amino acid(s)” refers to, for example, 1 to 16, 1 to 10, 1 to 9, 1to 8, 1 to 7, 1 to 6 (1 to several), 1 to 5, 1 to 4, 1 to 3, 1 or 2,or 1. A smaller number of the substituted amino acids is generally morepreferred. Such proteins may be obtained by using a site-specificmutagenesis technique described in, e.g., Sambrook J. et al., MolecularCloning: A Laboratory Manual, Third Edition, Cold Spring HarborLaboratory Press (2001); Ausbel F. M. et al, Current Protocols inMolecular Biology, Supplement 1-38, John Wiley and Sons (1987-1997);Nuc. Acids. Res., 10, 6487 (1982); Proc. Natl. Acad. Sci. USA, 79, 6409(1982); Gene, 34, 315 (1985); Nuc. Acids. Res., 13, 4431 (1985), Proc.Natl. Acad. Sci. USA, 82, 488 (1985); etc.

The positions of amino acids substituted in the amino acid sequence ofSEQ ID NO: 2 are not particularly limited as far as they are positionsother than the positions 107, 110, 120, 140, 179 and 180, and are one toseveral positions selected from positions 1 to 12, positions 47 to 103,and the like, preferably one to several positions selected from thegroup consisting of positions 4, 5, 6, 8, 11, 47, 49, 52, 53, 55, 56,59, 60, 61, 62, 64, 67, 68, 59, 71, 72, 74, 75, 76, 77, 78, 79, 81, 82,83, 84, 86, 87, 88, 91, 92, 93, 95, 96, 97, 98, 99, 101, 102 and 103.

In a particularly preferred embodiment of the present invention, theprotein is (a) a protein consisting of the amino acid sequence of SEQ IDNO: 2, (b) a protein comprising the amino acid sequence of SEQ ID NO: 2,and having the binding ability to the peroxide of coelenterazine or theperoxide of a coelenterazine derivative to form a holoprotein that emitslight by calcium ions, etc.

The protein of the invention may include an additional peptide sequenceat the N terminus and/or the C terminus, preferably at the N terminus.The additional peptide sequence includes, for example, at least onepeptide sequence selected from the group consisting of a peptidesequence for purification, a secretory signal peptide sequence and anepitope sequence recognizable by an antibody. The peptide sequence whichmay be additionally used is preferably a peptide sequence forpurification and/or a secretory signal peptide sequence. The peptidesequence for purification which may be used includes a peptide sequenceemployed in the technical field of the invention. Examples of thepeptide sequence for purification include a histidine tag sequencehaving a consecutive amino acid sequence of at least four, preferably atleast six, histidine residues, the amino acid sequence of theglutathione-binding domain in glutathione S-transferase and the aminoacid sequence of protein A. The term secretory signal peptide refers toa peptide region which plays the role of transporting the protein orpolypeptide bound to the secretory signal peptide across the cellmembrane. The amino acid sequences of such secretory signal peptides andnucleotide sequences encoding these peptides are well known and reportedin the relevant art (cf, e.g., von Heijine G (1988) Biochim. Biophys.Acta 947:307-333, von Heijine G (1990) J. Membr. Biol. 115: 195-201,etc). More specifically, secretory signal peptides include, for example,the secretory signal peptide from the outer membrane protein A from E.coli (OmpA) (Ghrayeb, J. et al., EMBO J. (1984), 3, 2437-2442) and thesecretory signal peptide from cholera toxin obtained from Vibriocholerae.

Methods for producing the protein of the invention are not particularlylimited. The protein of the invention may be a protein synthesized bychemicasl synthesis, or a recombinant protein produced by a geneticengineering technique. In chemically synthesizing the protein of theinvention, the protein may be synthesized by, for example, the Fmoc(fluorenylmethyloxycarbonyl) process, the tBoc (t-butyloxycarbonyl)process, etc. In addition, the peptide may be chemically synthesizedusing peptide synthesizers manufactured by Advanced ChemTech,PerkinElmer, Pharmacia, Protein Technology Instrument, Synthecell-Vega,PerSeptive, Shimadzu Corporation, etc. In producing the protein of theinvention by a genetic engineering technique, the protein may beproduced in a conventional manner by a genetic recombination technique.More specifically, the protein of the present invention may be producedby introducing a polynucleotide (e.g., DNA) encoding the protein of theinvention into a suitable expression system. The polynucleotide encodingthe protein of the invention and expression of the protein of theinvention in an expression system are described later.

The protein of the invention is brought in contact with luminescentsubstrate coelenterazine or a derivative thereof (e.g.,h-coelenterazine, e-coelenterazine, cl-coelenterazine,ch-coelenterazine, hcp-coelenterazine, etc.) in the presence of oxygen,whereby the holoprotein composed of the protein of the invention and theperoxide of coelenterazine or the peroxide of a coelenterazinederivative can be obtained. Hereinafter the “coelenterazine or aderivative thereof” is sometimes briefly referred to as“coelenterazine.” As used herein, the holoprotein composed of theprotein of the invention and the peroxide of coelenterazine or theperoxide of a coelenterazine derivative is sometimes referred to as “theholoprotein of the invention.” Herein, the “holoprotein (photoprotein)of the invention” is used to mean a complex (holoprotein) comprising theprotein of the invention (apoprotein) and the peroxide of coelenterazineor the peroxide of a coelenterazine derivative, Examples of theholoprotein of the invention include a holoprotein composed of theprotein of the invention and the peroxide of coelenterazine, aholoprotein composed of the protein of the invention and the peroxide ofa coelenterazine derivative, and the like. Examples of the holoproteincomposed of the protein of the invention and the peroxide of acoelenterazine derivative include a holoprotein composed of the proteinof the invention and the peroxide of h-coelenterazine, a holoproteincomposed of the protein of the invention and the peroxide ofe-coelenterazine, a holoprotein composed of the protein of the inventionand the peroxide of n-coelenterazine, a holoprotein composed of theprotein of the invention and the peroxide of ch-coelenterazine, aholoprotein composed of the protein of the invention and the peroxide ofhcp-coelenterazine, and the like. The holoprotein of the invention canbe produced from the protein of the invention and the coelenterazine inthe same manner as with known calcium-binding photoproteins (e.g.,aequorin, etc.). More specifically, the holoprotein of the invention canbe produced by methods described in, for example, Shimomura, O. et al.,(1988) Biochem. J., 251, 405-410; Shimomura, O. et al., Biochem, J.(1989) 261, 913-920, etc. The holoprotein of the invention exists in thepresence of oxygen, in the state of a complex of the protein of theinvention and the peroxide of coelenterazine which is formed fromcoelenterazine and molecular oxygen. When calcium ions bind to thiscomplex, a flash of light is emitted to form coelenteramide as the oxideof coelenterazine and carbon dioxide. This complex (holoprotein of theinvention) is sometimes referred to as the “photoprotein of theinvention,”

2. Polynucleotide of the Invention

The present invention further provides a polynucleotide encoding theprotein of the invention described above. The polynucleotide of theinvention may be any polynucleotide so long as it has a nucleotidesequence encoding the protein of the invention, preferably a DNA.Examples of the DNA include genomic DNA, genomic DNA library, cDNAderived from cells or tissues, cDNA library derived from cells ortissues, synthetic DNA, etc. The vectors used in these libraries are notparticularly limited and may be any of bacteriophages, plasmids, cosmidsand phagemids. The polynucleotide may also be amplified directly by areverse transcription polymerase chain reaction (hereinafter abbreviatedas RT-PCR) using total RNA or a mRNA fraction prepared from the cells ortissues described above.

The polynucleotide of the present invention includes:

(a) a polynucleotide comprising a polynucleotide consisting of thenucleotide sequence of SEQ ID NO: 1;

(b) a polynucleotide comprising a polynucleotide encoding the proteinconsisting of the amino acid sequence of SEQ ID NO: 2;

(c) a polynucleotide comprising a polynucleotide encoding a proteinconsisting of the amino acid sequence of SEQ ID NO. 2, wherein the aminoacids at positions 107, 110, 120, 140, 179 and 180 are aspartic acid,aspartic acid, glycine, proline, threonine and serine, respectively, andone to several amino acid(s) except for the amino acid(s) at thepositions above are substituted with other amino acid(s), and havingsubstantially the same activity or function as the protein consisting ofthe amino acid sequence of SEQ ID NO: 2;

(e) a polynucleotide comprising a polynucleotide encoding a proteincomprising the amino acid sequence of SEQ ID NO: 2, and havingsubstantially the same activity or function as the protein consisting ofthe amino acid sequence of SEQ ID NO: 2;

(f) a polynucleotide comprising a polynucleotide encoding a proteincomprising the amino acid sequence of SEQ ID NO. 2, wherein the aminoacids at positions 107, 110, 120, 140, 179 and 180 are aspanic acid,aspartic acid, glycine, proline, threonine and serine, respectively, andone to several amino acid(s) except for the amino acid(s) at thepositions above are substituted with other amino acid(s), and havingsubstantially the same activity or function as the protein consisting ofthe amino acid sequence of SEQ ID NO: 2; and the like.

Examples of the polynucleotide comprising a polynucleotide consisting ofthe nucleotide sequence of SEQ ID NO: 1 include:

(a) a polynucleotide consisting of the nucleotide sequence of SEQ ID NO:1, 3 or 5;

(b) a polynucleotide comprising a polynucleotide consisting of thenucleotide sequence of SEQ ID NO: 1, 3 or 5; and the like.

The substantially the same activity or function is as definedhereinabove

The term “amino acid sequence in which one to several amino acid(s) aresubstituted” is also as defined hereinabove.

The polynucleotide encoding a protein having, with respect to a givenamino acid sequence, one to several amino acids being substituted can beobtained using a site-specific mutagenesis technique (see, for example,Gotoh, T. et al., Gene, 152, 271-275 (1995); Zoller, Mi., and Smith, M.,Methods Enzymol., 100, 468-500 (1983); Kramer, \V. et al., Nucleic AcidsRes., 12, 9441-9456 (1984); Kramer W, and Fritz H. J., Methods. Enzymol.154, 350-367 (1987); Kunkel, T. A., Proc. Natl. Acad. Sci. USA., 82,488-492 (1985), Kunkel, Methods Enzymol., 85, 2763-2766 (1988); etc.),and methods using amber mutation (see, for example, the gapped duplexmethod described in Nucleic Acids Res., 12, 9441-9456 (1984), etc.).

Alternatively, a mutation can be introduced into the polynucleotide byPCR using a set of primers bearing on the respective 5′ ends a sequencein which the target mutation (deletion, addition, substitution and/orinsertion) is introduced (see, for example. Ho, S, N. et al., Gene, 77,51 (1989), etc.)

Furthermore, a polynucleotide encoding a partial fragment of protein,which is one type of deletion mutants, can be obtained by PCR using asthe primers an oligonucleotide having a sequence that matches thenucleotide sequence at the 5′ end of the region encoding the targetpartial fragment in a polynucleotide encoding the protein and anoligonucleotide having a sequence complementary to the nucleotidesequence at the 3′ end, and using the polynucleotide encoding theprotein as a template.

Preferably, the polynucleotide of the present invention is, for example,a polynucleotide comprising a polynucleotide consisting of thenucleotide sequence of SEQ ID NO: 1, a polynucleotide comprising apolynucleotide encoding a protein consisting of the amino acid sequenceof SEQ ID NO: 2, a polynucleotide comprising a polynucleotide encoding aprotein comprising the amino acid sequence of SEQ ID NO: 2 and havingsubstantially the same activity or function as the protein consisting ofthe amino acid sequence of SEQ ID NO: 2, and the like.

The polynucleotide of the present invention may further contain apolynucleotide encoding an additional peptide sequence at the 5′ endand/or 3′ end, preferably at the 5′ end. The polynucleotide encoding theadditional peptide sequence may include, for example, at least onepeptide sequence selected from the group consisting of a peptidesequence for purification, a secretory signal peptide sequence, etc. Thepeptide sequence for purification which may be used includes a peptidesequence employed in the technical field of the invention. The peptidesequence for purification includes those described above. Thepolynucleotide encoding a secretory signal peptide which may be usedincludes a polynucleotide comprising a nucleic acid sequence encoding asecretory signal peptide known in the art. The secretory signal peptideincludes those described above.

3. Recombinant Vector and Transformant of the Invention

The present invention further provides a recombinant vector comprisingthe polynucleotide of the invention described above and a transformant.

(1) Construction of Recombinant Vector

The recombinant vector of the present invention can be obtained byligating (inserting) the polynucleotide (DNA) of the invention into asuitable vector. More specifically, the recombinant vector can beobtained by cleaving a purified form of the polynucleotide (DNA) with asuitable restriction enzyme and inserting the cleavage product into arestriction enzyme site or multicloning site on a suitable vector,thereby ligating the polynucleotide to the vector. The vector forinserting the polynucleotide of the invention is not particularlylimited, as far as the vector is capable of replication in a host.Vectors which may be used include plasmids, bacteriophages, animalviruses, etc. Examples of such plasmids include plasmids from E. coli(e.g., pBR322, pBR325, pUC118, pUC119, etc.), plasmids from Bacillussubtilis (e.g., pUB110, pTP5, etc.), and plasmids from yeast (e.g.,YEp13, YEp24, YCp50, etc.). An example of the bacteriophage is a λphage. Examples of the animal viruses include retroviruses, vacciniaviruses and insect viruses (e.g., baculoviruses, etc.).

The polynucleotide of the present invention is generally ligateddownstream from the promoter of a suitable vector in such a manner thatit can be expressed. Where the host used for transformation is an animalcell, preferred examples of the promoter used include a promoter fromSV40, a retrovirus promoter, a metallothionein promoter, a heat shockpromoter, a cytomegalovirus promoter, a SRa promoter, etc. Where thehost is a bacterium belonging to the genus Escherichia, preferredexamples of the promoter include a Trp promoter, T7 promoter, lacpromoter, recA promoter, λPL promoter and 1 pp promoter, etc. Where thehost is a bacterium belonging to the Bacillus, preferred examples of thepromoter include a SPO1 promoter, SPO2 promoter and the penP promoter.If the host is a yeast, preferred promoters include the PHO5 promoter,the PGK promoter, the GAP promoter, the ADH1 promoter and GAL promoter,etc. Where the host is an insect cell, preferred examples of thepromoter include a polyhedrin promoter and P10 promoter, etc.

In addition to those described above, the recombinant vector of thepresent invention which can be used include those containing, ifdesired, an enhancer, a splicing signal, a poly(A) addition signal, aribosome binding sequence (SD sequence), a selective marker and thelike. Examples of the selective marker include a dihydrofolate reductasegene, ampicillin resistance gene and neomycin resistance gene.

(2) Preparation of Transformant

The transformant can be prepared by introducing the recombinant vectorcomprising the polynucleotide of the invention thus obtained (i.e., thepolynucleotide encoding the protein of the invention) into a suitablehost. The host is not particularly limited, so long as it is capable ofexpressing the polynucleotide (DNA) of the invention. Examples of thehost include bacteria belonging to the genera Escherichia, Bacillus,Pseudomonas and Rhizobium, yeasts, animal cells or insect cells, etc.Bacteria of the genus Escherichia include Escherichia coli, etc.Bacteria of the genus Bacillus include Bacillus subtilis, etc. Bacteriaof the genus Pseudomonas include Pseudomonas putida, etc. Bacteria ofthe genus Rhizobium include R. meliloti, etc. Yeasts includeSaccharomyces cerevisiae, Schizosaccharomyces pombe, etc. Animal cellsinclude COS cells, CHO cells, etc. Insect cells include Sf9, Sf21, etc.

Introduction of the recombinant vector into the host and transformationthereby can be performed by various methods generally used in the art.Examples of suitable methods for introducing the recombinant vector intohost cells include the calcium phosphate method (Virology, 52, 456-457(1973)), lipofection (Proc. Natl. Acad. Sci. USA, 84, 7413 (1987)),electroporation (EMBO J., 1, 841-845 (1982)), etc. Examples of methodsfor transforming bacteria of the genus Escherichia include the methodsdescribed in Proc. Natl. Acad. Sci. USA, 69, 2110 (1972), Gene, 17, 107(1982), etc. Methods for transforming bacteria of the genus Bacillusinclude the methods described in Molecular & General Genetics, 168, 111(1979), etc. Methods for transforming yeasts include the methodsdescribed in Proc. Natl. Acad. Sci. USA, 75, 1929 (1978), etc. Methodsfor transforming animal cells include the methods described in Virology,52, 456 (1973), etc. Methods for transforming insect cells include themethods described in Bio/Technology, 6, 47-55 (1988), etc. Thus, thetransformant prepared by transformation with the recombinant vectorcomprising the polynucleotide encoding the protein of the invention(i.e., the polynucleotide of the invention) can be obtained.

4. Production of Protein of the Invention

The present invention further provides a method of producing the proteinof the invention, which comprises the step of culturing the transformantdescribed above to produce the protein of the invention. The protein ofthe invention can be produced by culturing the transformant above underconditions where the polynucleotide (DNA) encoding the protein of theinvention can be expressed, to produce and accumulate the protein of theinvention, and isolating and purifying the protein.

(Incubation of Transformant)

The transformant of the invention can be cultured in a conventionalmanner used for incubation of hosts. By the incubation, the protein ofthe invention is produced using the transformant and accumulated withinthe transformant or in the culture broth.

The medium for culturing the transformant, which is used to incubatebacteria of the genus Escherichia or Bacillus as the host, may be any ofa natural medium or a synthetic medium, so long as it is a mediumcontaining carbon sources, nitrogen sources, inorganic salts and othernutrients essential for growth of the transformant where thetransformant can be efficiently grown. Examples of the carbon sourceswhich can be used include carbohydrates such as glucose, fructose,sucrose, starch, etc.; organic acids such as acetic acid, propionicacid, etc.; and alcohols such as ethanol, propanol, etc. Examples of thenitrogen sources which can be used include ammonia, ammonium salts ofinorganic or organic acids, such as ammonium chloride, ammonium sulfate,ammonium acetate, ammonium phosphate, etc., other nitrogen-containingcompounds, and further include peptone, meat extract, corn steep liquor,etc. Examples of the inorganic salts that can be used include potassium(I) phosphate, potassium (II) phosphate, magnesium phosphate, magnesiumsulfate, sodium chloride, ferrous sulfate, manganese sulfate, coppersulfate, calcium carbonate, etc. If necessary, antibiotics such asampicillin or tetracycline may be added to the medium during culturing.Where the transformant transformed by an expression vector using aninducible promoter as the promoter is cultured, an inducer may also beadded to the medium if necessary. For example,isopropyl-β-D-thiogalactopyranoside (IPTG), etc. may be added to themedium when a transformant transformed by an expression vector using aLac promoter is cultured, and when a transformant transformed by anexpression vector using a trp promoter is cultured, indoleacrylic acid(IAA), etc. may be added to the medium.

When the host is a bacterium of the genus Escherichia, incubation isperformed generally at approximately 15 to 43° C. for approximately 3 to24 hours. Aeration or stirring may be applied depending upon necessity.When the host is a bacterium of the genus Bacillus, incubation iscarried out generally at approximately 30 to 40° C. for approximately 6to 24 hours. Aeration or stirring may be applied depending uponnecessity.

Media for culturing the transformant when the host is yeast includeBurkholder's minimal medium (Proc. Natl. Acad, Sci. USA, 77, 4505(1980)), a SD medium containing 0.5% (w/v) casamino acids (Proc. Natl.Acad. Sci. USA, 81, 5330 (1984)), etc. The pH of the medium ispreferably adjusted to approximately 5 to 8. Culture is generallycarried out at approximately 20 to 35° C. for approximately 24 to 72hours. Aeration or stirring may be applied, depending upon necessity.

Media for culturing the transformant when the host is an animal cellinclude MEM medium containing approximately 5 to 20% (v/v) fetal calfserum (Science, 122, 501 (1952)), DMEM medium (Virology, 8, 396 (1959)),etc. The pH of the medium is preferably adjusted to approximately 6 to8. Culture is generally carried out at approximately 30 to 40° C. forapproximately 15 to 60 hours. Aeration or stirring may be applied,depending upon necessity.

Media for culturing the transformant when the host is an insect cellinclude Grace's insect medium (Nature, 195, 788 (1962)) suitablysupplemented with additives such as 10% (v/v) immobilized bovine serum.The pH of the medium is preferably adjusted to approximately 6.2 to 6.4.Culture is generally carried out at approximately 27° C. forapproximately 3 to 5 days, Aeration or stirring may be applied,depending upon necessity.

(Isolation and Purification of Protein of the Invention)

The protein of the invention can be obtained by isolating and purifyingthe protein of the invention from the culture above. As used herein, theculture refers to any one of a culture broth, cultured bacterial cellsor cultured cells, and the homogenates of cultured bacterial cells orcultured cells. The isolation and purification of the protein of theinvention can be performed in a conventional manner.

Specifically, when the protein of the invention is accumulated withincultured bacterial cells or within cultured cells, after the completionof cultivation, the bacterial cells or cells are disrupted in aconventional manner (e.g., ultrasound, lysozymes, freezing and thawing)and a crude extract of the protein of the present invention can beobtained in a conventional manner (e.g., centrifugation, filtration,etc.). When the protein of the invention is accumulated in theperiplasmic space, after the completion of cultivation, an extractcontaining the target protein can be obtained in a conventional manner(e.g., osmotic shock, etc.). When the protein of the invention isaccumulated in the culture broth, after the completion of cultivation,the bacteria or cells are separated from the culture supernatant in aconventional manner centrifiigation, filtration, etc.), whereby theculture supernatant containing the protein of the invention can beobtained.

The protein of the present invention in the extract or culturesupernatant thus obtained can be purified by a conventional method ofseparation and purification. Examples of the separation and purificationmethods include ammonium sulfate precipitation, gel filtrationchromatography, ion-exchange chromatography, affinity chromatography,reversed phase high performance liquid chromatography, dialysis,ultrafiltration, etc., which may be used solely or in a suitablecombination. Where the protein of the invention contains theabove-described peptide sequence for purification, it is preferred touse the same for purification. Specifically, where the protein of theinvention contains a histidine-tagged sequence, nickel chelate affinitychromatography can be used, in the protein of the invention whichcontains the glutathione-binding domain of S-transferase, affinitychromatography using a glutathione-binding gel can be used; and, in theprotein of the invention which contains the amino acid sequence ofProtein A, antibody affinity chromatography can be used.

The holoprotein (photoprotein) of the invention which emits lightdependently on the calcium ion concentration can be prepared byincubation of the purified apoprotein of the invention together with theluminescent substrate coelenterazine or its derivative at a lowtemperature in the presence of a reducing agent (e.g., mercaptoethanol,dithiothreitol, etc.) and oxygen,

5. Uses of Protein of the Invention

(Detection and Quantification of Calcium Ions)

As described above, the protein (apoprotein) of the invention is aprotein which can be produced by forming a non-covalent bond with theperoxide of coelenterazine or the peroxide of a coelenterazinederivative, which is formed from coelenterazine or its derivative andmolecular oxygen, and can form a holoprotein (photoprotein) which emitslight by calcium ions. The protein of the invention and the holoproteinof the invention can be used for detecting or quantifying calcium ions.

When the protein of the invention is used to detect or quantify calciumions, the holoprotein composed of the protein (apoprotein) of theinvention and the peroxide of coelenterazine or the peroxide of acoelenterazine derivative is used. The holoprotein described above canbe produced by the method described above. The detection orquantification of calcium ions can be performed by adding a samplesolution directly to a solution of the holoprotein and measuring theluminescence generated. The detection or quantification of calcium ionscan also be performed by adding a solution of the holoprotein to asample solution and measuring the luminescence generated. Alternatively,prior to the addition in the measurement system for detection orquantification of calcium ions, an aqueous solution of the protein(apoprotein) of the invention is previously brought in contact withcoelenterazine or its derivative (e.g., h-coelenterazine,e-coelenterazine, cl-coelenterazine, ch-coelenterazine,hep-coelenterazine, etc.) and the holoprotein thus formed may be used.Furthermore, the protein (apoprotein) of the invention may also bebrought in contact with coelenterazine or its derivative in themeasurement system to form a holoprotein composed of the protein of theinvention and the peroxide of coelenterazine or the peroxide of acoelenterazine derivative. The holoprotein thus formed is a complex(photoprotein) of the protein (apoprotein) of the invention and theperoxide of coelenterazine or the peroxide of a coelenterazinederivative; the aforesaid complex (i.e., the holoprotein of theinvention) emits light dependently on the calcium ion concentration.Accordingly, the protein (apoprotein) of the invention or theholoprotein of the invention can be used to detect calcium ions.Specifically, the calcium ions can be detected by adding a samplesolution directly to a solution of the holoprotein and measuring theluminescence generated, as described above. Alternatively, the calciumions can be detected by adding a solution of the holoprotein to a samplesolution and then measuring the luminescence generated.

The detection or quantification of calcium ions can be performed bymeasuring the luminescence of the holoprotein of the invention bycalcium ions using a luminometer. Luminometers which can be used includecommercially available instruments such as Centro LB 960 (manufacturedby Berthold), etc. The calcium ion concentration can be quantitativelydetermined by preparing a luminescence standard curve for known calciumion concentrations using the holoprotein.

The protein of the invention may also be used to detect changes in theconcentration of intracellular calcium ions under physiologicalconditions, by constructing a holoprotein composed of the protein of theinvention and the peroxide of coelenterazine or the peroxide of acoelenterazine derivative, and directly introducing the holoprotein intothe cell by means of microinjection, etc.

In addition to the introduction into a cell by means of microinjection,etc., the protein of the invention may be formed intracellularly byintracellularly expressing an apoprotein gene (a polynucleotide encodingthe protein of the invention). The holoprotein may also be formed byadding coelenterazine or its derivative to the protein (apoprotein) ofthe invention thus formed from outside the cell.

Using the holoprotein of the invention thus introduced into or formedwithin the cell, changes in the concentration of intracellular calciumions in response to external stimuli (e.g., stimuli with a drug which isassociated with a receptor) can also be measured.

(Use as Reporter Protein)

The protein of the invention can be used also as a reporter protein toassay the transcription activity of a promoter or the like. Thepolynucleotide encoding the protein of the invention (i.e., thepolynucleotide of the invention) is fused to a target promoter or someother expression control sequence (e.g., an enhancer, etc.) to constructa vector. The resulting vector is introduced into a host cell and theluminescence generated from the protein of the invention (i.e., theluminescence by the holoprotein of the invention) is detected. Thus, theactivity of the target promoter or some other expression controlsequence can be assayed.

As described above, the polynucleotide of the invention can be used as areporter gene

(Use as Marker for Detection by Luminescence)

The protein of the invention can be used as a marker for detection byluminescence. The detection marker of the invention is available for thedetection of a target substance in, for example, an immunoassay orhybridization assay. The holoprotein of the invention can be used bybinding the same to a target protein or a target nuclei acid in aconventional manner such as chemical modifications. Such detectionmarkers can be used for the detection in a conventional manner. Thedetection marker of the invention can also be used to determine thedistribution of a target protein by expressing the marker as a fusionprotein to the target protein and inserting the fusion protein into acell by means of microinjection, etc. The distribution of a targetprotein described above can be determined by a method for detection suchas luminescence imaging. The protein of the invention can also be usedafter expression of the protein in a cell, in addition to the insertioninto a cell by means of microinjection, etc.

(Material for Amusement Product)

The complex composed of the protein of the invention and the peroxide ofcoelenterazine or the peroxide of a coelenterazine derivative (thecomplex is the holoprotein of the invention) emits light merely bybinding to a trace amount of calcium ions. The luminescence intensity ofthe complex (the holoprotein of the invention) above is at least fivetimes greater than that of the known photoprotein clytin-I. Therefore,the protein of the invention, the holoprotein of the invention and thelike can be suitably used as a luminescent substrate in materials foramusement products. Examples of amusement products include luminescentbubble soap, luminescent ice, luminescent candies and luminescentpaints. The amusement products of the invention can be prepared in aconventional manner.

6. Kit of the Invention

The present invention further provides a kit comprising any of theprotein of the invention, the holoproteins of the invention, thepolynucleotide of the invention, the recombinant vector of the inventionand the transformant of the invention. The kit of the invention mayadditionally contain coelenterazine or a derivative thereof. The kit ofthe invention can be prepared according to conventional methods usingconventional materials. The kit of the invention may also contain sampletubes, plates, instructions for the user, solutions, buffers, reagents,and either samples suitable for standardization or control samples.

The kit of the present invention can be used for the detection orquantification of calcium ions described above, the measurement using areporter protein or a reporter gene, as a fluorescent marker, or thelike.

7. Fluorescent Protein

7.1 Method of Producing Fluorescent Protein

The fluorescent protein produced by the method of producing thefluorescent protein of the invention is a complex in whichcoelenteramide or its analog is coordinated to the protein of theinvention. The fluorescent protein of the invention can emitfluorescence under the excitation of light. In some embodiments, thefluorescent protein of the invention has both bioluminescence andfluorescence spectrum, wherein, for example, the fluorescence maximumwavelength is shifted toward a longer wavelength region than theluminescence maximum wavelength.

In the present invention, the fluorescent protein is produced fromcoelenteramide or its analog by the following procedures. In moredetail, the fluorescent protein is produced by reacting the protein ofthe invention with coelenteramide or its analog in the presence orabsence of calcium ions or divalent or trivalent ions that can besubstituted for the calcium ions.

In the present invention, coelenteramide or its analog which is used toproduce the fluorescent protein includes the compounds described in thepamphlet of WO 2005/014633, page 6, line 15 to page 7, line 23, thecompounds represented by general formula (1) below, and the like.

Compounds represented by the formula below.

(wherein

R¹ is a substituted or unsubstituted aryl, a substituted orunsubstituted arylalkyl, a linear or branched alkyl which may optionallybe substituted with an alicyclic group, an alicyclic group or aheterocyclic group;

R² is hydrogen or —(SO₂)R⁴;

R³ is hydrogen, hydroxy group, methoxy or acetoxy; and,

R⁴ is substituted or unsubstituted aryl, a substituted or unsubstitutedarylalkyl or a linear or branched alkyl which may optionally besubstituted with an alicyclic group; and,

X¹ is —C(═S)— or —SO₂—).

Herein, in general formula (1), it is preferred that R¹ is phenyl,p-methylphenyl, p-hydroxyphenyl, p-methoxyphenyl, p-acetoxyphenyl,p-nitrophenyl, benzyl, α-hydroxybenzyl, 4-methylbenzyl, 4-hydroxybenzyl,4-methoxybenzyl, 4-acetoxybenzyl, 4-nitrobenzyl, phenylethyl, methyl,ethyl, propyl, 2-methylpropyl, 2-methylpropanyl, cyclohexylmethyl,cyclohexylethyl, adamantylmethyl, cyclopentylmethyl, cyclohexyl orthiophen-2-yl.

Further in general formula (1), it is preferred that R² is hydrogen,benzenesulfonyl, p-toluenesulfonyl, 4-hydroxyphenylsulfonyl,4-methoxyphenylsulfonyl, 4-acetoxyphenylsulfonyl, 4-nitrophenylsulfonyl,benzylsulfonyl, α-hydroxybenzylsulfonyl, 4-methylbenzylsulfonyl,4-hydroxybenzylsulfonyl, 4-methoxybenzylsulfonyl,4-acetoxybenzylsulfbnyl, 4-nitrobenzylsulfonyl, phenylethylsulfonyl,methanesulfonyl, ethylsulfonyl, propylsulfonyl, 2-methylpropylsulfonyl,2-methylpropanylsulfonyl, cyclohexylmethylsulfonyl,cyclohexylethylsulfonyl, adamantylmethylsulfonyl orcyclopentylmethylsulfonyl.

In the present invention, coelenteramide or its analog which is used toproduce the fluorescent protein includes the compounds described in thepamphlet of WO 2005/014633, page 42, line 19 to page 130, line 1, thecompounds selected from the group consisting of the following compounds,and the like.

More preferred examples of the coelenteramide or its analog which isused to produce the fluorescent protein in the present invention includecoelenteramide, e-coelenteramide and ch-coelenteramide

The coelenteramide or its analog can be produced by, for example, themethod described in REFERENCE EXAMPLE 1 later given, the methoddescribed in Shimomura & Johnson, Tetrahedron Lett. (1973) 2963-2966,the method described in Teranishi & Goto, Bull, Chem, Soc. Jpn (1990)63:3132-3140, the method described in Shimomura & Teranishi,Luminescence (2000) 15:51-58, or modifications of these methods.

Herein, in the compounds represented by general formula (1), thecompound represented by general formula (2) below:

(wherein R¹, R² and R³ are as defined above) can be produced by reactingthe compound represented by general formula (4):

(wherein R³ is as defined above) with the compound represented bygeneral formula (5):

(wherein R¹ is as defined above).

The compound represented by general formula (4) can be produced by knownprocesses. For example, the compound represented by general formula (4)can be produced by, for example, the methods described in Kishi, Y. etal., Tetrahedron Lett., 13, 2747-2748 (1972) or Adamczyk, M. et al.,Org. Prep. Proced. Int., 33, 477-485 (2001), or modifications of thesemethods. More specifically, the compound represented by general formula(4) can be prepared as follows. First, cyclization of a substitutedphenylglyoxal aldoxime and a glycinonitrile derivative is carried outusing a Lewis acid catalyst such as titanium tetrachloride to form thepyrazine oxide. Subsequently, the pyrazine oxide is subjected tocatalytic hydrogen reduction using Raney Ni, etc, as a catalyst toproduce the compound. Alternatively, the compound can be producedthrough the Suzuki-Miyaura coupling reaction of a2-amino-5-bromopyrazine derivative and a substituted phenyl pinacolboronate ester.

The compound represented by general formula (5) can be produced by knownprocesses or is commercially available. Specifically, the compound canbe produced by, for example, 1) reacting the corresponding substitutedbenzylsulfonic acid or its salt with an excess of thionyl chloride andheating the reaction mixture under reflux, followed by concentrationunder reduced pressure, or 2) reacting the corresponding substitutedbenzylsulfonic acid or its salt with the corresponding carboxylic acidchloride obtained by the treatment with oxalyl dichloride in a solventsuch as dichloromethane in the presence of a catalytic amount ofN,N-dimethylformamide (DMF) followed by concentration under reducedpressure, or 3) reacting a substituted benzyl Grignard reagent withsulfuryl chloride, or modifications thereof. Benzylsulfonic chloride canbe purchased from Tokyo Chemical Industry Co., Ltd., Wako Pure ChemicalIndustries, Ltd., Kanto Chemical Co., Inc., etc.

Herein, the solvent used for the process of producing the compoundrepresented by general formula (2) is not particularly limited andvarious solvents can be used, except for aqueous or alcoholic solvents.Examples of the solvent include pyridine, dichloromethane, chloroform,acetonitrile, tetrahydrofuran, ethyl acetate, acetone, toluene, dioxan,ether, and the like. These solvents can be used alone or as an admixturethereof.

In the process of producing the compound represented by general formula(2), the reaction temperature and reaction time are not particularlylimited and include, for example, −20° C. to 200° C. for 0.25 to 72hours, preferably −20° C. to 100° C. for 0.5 to 36 hours, and morepreferably, 0° C. to 50° C. for an hour to 24 hours.

Furthermore, in the compounds represented by general formula (2), somecompounds wherein R² is H, can be produced through alkali hydrolysis ofthe compound represented by R²═SO₂R¹, i.e., the disulfonic amidecompound to selectively cleave the sulfonic amide bond on one side only,or by modifications thereof.

In the compounds represented by general formula (1), the thioamidecoelenteramide represented by general formula (3):

(wherein R¹, R² and R³ are as defined above), can be produced by, e.g.,reacting the compound represented by general formula (6):

with Lawesson's reagent or phosphorus pentasulfide (tetraphosphorusdecasulfide).

The compound represented by general formula (6) can be produced by knownmethods for production. Specifically, the compound can be produced by,e.g., reacting the compound represented by general formula (4) and theacid halide represented by general formula (7) or an analog thereof:

(wherein R¹ is as defined above and X is a halogen (e.g., fluorine,chlorine, bromine or iodine) or R¹C(═O)—) either in an organic solventin the presence of a base, or in a basic organic solvent, or bymodifications thereof.

Herein, the solvent used in the process of producing the compoundrepresented by general formula (3) is not particularly limited unless itis an aqueous, alcohol, ketone and ester solvent. Examples of thesolvent include toluene, benzene, dioxan, tetrahydrofuran, ether,dichloromethane, chloroform, pyridine and the like, which can be usedalone or as an admixture thereof.

Further in the process of producing the compounds represented by generalformula (3), the reaction temperature and reaction time are notparticularly limited and include, for example, 0° C. to 200° C. for 0.5to 72 hours, preferably room temperature to 200° C. for 1 to 48 hours,and more preferably, 60° C. to 150° C. for 2 to 24 hours.

The amount of coelenteramide or its analog used for producing thefluorescent protein is not particularly limited and is, for example, 1mol to 5 mol, preferably 1 mol to 2 mol, and more preferably 1 mol to1.2 mol, per mol of the protein of the invention.

In some embodiments of the present invention, divalent or trivalent ionsthat can be substituted for the calcium ions are used to produce thefluorescent protein. As used herein, the divalent or trivalent ions thatcan be substituted for the calcium ions refer to divalent or trivalentions which cause a luminescence reaction when they are reacted with thecalcium-binding photoprotein in place of calcium ions. In other words,the ions refer to ions that exert the similar function to calcium ionson a calcium-binding photoprotein. Examples of such ions include calciumions (Ca²⁺), magnesium ions (Mg²⁺), strontium ions (SR²⁺), barium ions(Ba²⁺), lead ions (Pb²⁺), cobalt ions (Co²⁺), nickel ions (Ni²⁺) cadmiumions (Cd²⁺), yttrium ions (Y³⁺), lanthanum ions (La³⁺), samarium ions(Sm³⁺), europium ions (Eu³⁺), dysprosium ions (Dy³⁺), thulium ions(Tm³⁺), and yttribium ions (Yb³⁺). Of these ions, divalent metal ionsare preferred and divalent ions of metals other than transition metals(e.g., Ca²⁺, SR²⁺ and Pb²⁺) are more preferred.

Where calcium ions or the divalent or trivalent ions that can besubstituted for the calcium ions are used, the amount is notparticularly limited and is, for example, 4 mol to 10 mol, 10 mol to 100mol, 100 mol to 1000 mol, etc., per mol of the protein of the invention.

In the production of the fluorescent protein of the invention, thereaction of the protein of the invention with coelenteramide and itsanalog is preferably carried out in the presence of a reducing agent.Examples of the reducing agent used herein include dithiothreitol (DTT),mercaptoethanol and the like. The amount of the reducing agent used toproduce the fluorescent protein of the invention is not particularlylimited unless it affects the reconstitution of the fluorescent proteinof the invention. When two or more cysteine residues are present in theprotein of the invention, the reducing agent is preferably set at aconcentration so as to prevent S—S bond formation. For example, 1 mMdithiothreitol or 0.1% mercaptoethanol is preferred.

In some embodiments of the present invention, the reaction between theprotein of the invention and coelenteramide or its analog is carried outin the presence of a chelating agent to remove calcium ions or thedivalent or trivalent ions that can be substituted for the calcium ions.In this case, the amount of the chelating agent is not particularlylimited unless it affects production of the fluorescent protein. It isshown that 3 mol of calcium ions are bound to 1 mol of the protein ofthe invention in its ionic state. Therefore, it is preferred to use atleast 3 mol of the chelating agent.

The chelating agent used to produce the fluorescent protein may be anyone and is not particularly limited, so long as it strongly hinds tocalcium ions or the divalent or trivalent ions that can be substitutedfor the calcium ions. Examples of the chelating agent includeethylenediaminetetraacetic acid (EDTA), ethyleneglycol bis(β-aminoethylether)-N,N,N′,N′-tetraacetic acid (EGTA),trans-1,2-diaminocyclohexane-N,N,N′,N′-tetraacetic acid (CyDTA),N-(2-hydroxyethyl)iminodiacetic acid (HIDA), and the like.

In the production of the fluorescent protein, the reaction temperatureand reaction time are not particularly limited and include, for example,0° C. to 42° C. for 0.1 to 2 hours, 4° C. to 37° C. for 0.1 to 2 hours,or 4° C. to 15° C. for 0.1 to 24 hours.

The fluorescent protein thus obtained may be further purified. Thepurification of gFP can be performed by conventional methods forseparation/purification. Examples of methods for separation/purificationinclude ammonium sulfate precipitation, gel filtration chromatography,ion-exchange chromatography, affinity chromatography, reversed phasehigh performance liquid chromatography, dialysis, ultrafiltration, etc.,which may be used solely or in a suitable combination.

7.2. Use of Fluorescent Protein

(1) Use as Reporter Protein

The fluorescent protein of the invention can be used also as a reporterprotein to assay the transcription activity of a promoter or the like.For example., the polynucleotide encoding the protein of the inventionis fused to a target promoter or some other expression control sequence(e.g., an enhancer, etc.) to construct a vector. The resulting vector isintroduced into a host cell, with which coelenteramide or its analog isbrought in contact in the presence or absence of calcium ions or thedivalent or trivalent ion that can be substituted for the calcium ionsto produce the fluorescent protein. By detecting the fluorescencegenerated from the fluorescent protein of the invention, the activity ofthe target promoter or some other expression control sequence can beassayed

(2) Use as Marker for Detection

The fluorescent protein of the invention can be used as a marker fordetection by fluorescence. The detection marker is available for thedetection of a target substance in, for example, an immunoassay orhybridization assay. The fluorescent protein can be used by binding to atarget substance (a protein or a nuclei acid) in a conventional mannersuch as chemical modifications. Such detection markers can be used forthe detection in a conventional manner. The detection marker of theinvention can also be used to determine the distribution of a targetprotein by expressing the marker as a fusion protein to the targetsubstance, inserting the fusion protein into a cell by means ofmicroinjection, etc. and further bringing coelenteramide or its analogin contact therewith in the presence or absence of calcium ions or thedivalent or trivalent ion that can be substituted for the calcium ionsthereby to form the fluorescent protein. The distribution of a targetsubstance can be determined by a method for detection such asfluorescence imaging. The apoprotein can also be used after expressionin a cell, in addition to the insertion into a cell by means ofmicroinjection, etc.

(3) Material for Amusement Product

The fluorescent protein of the invention can be suitably used as afluorescent substrate in materials for amusement products. Examples ofamusement products include fluorescent bubble soap, fluorescent ice,fluorescent candies and fluorescent paints. The amusement products canbe prepared in a conventional manner

Where no particular explanation is given for the embodiments or examplesto carry out the invention, there may be used the methods described instandard protocols such as J. Sambrook, E. F Fritsch & T. Maniatis(Ed.), Molecular Cloning, A Laboratory Manual (3^(rd) edition), ColdSpring Harbor Press, Cold Spring Harbor, New York (2001); F. M. Ausubel,R. Brent, R. E. Kingston, D. D. Moore, J. O, Seidman, J. A. Smith, K,Struhl (Ed.), Current Protocols in Molecular Biology, John Wiley & SonsLtd.; or modifications or variations thereof. When commerciallyavailable reagent kits and measurement equipments are used, theprotocols attached thereto are used, unless otherwise indicated.

All literatures and publications mentioned in this specification areherein incorporated in their entirety by reference into thespecification, irrespective of their purposes. This specificationincludes all of the contents as disclosed in the claims, specificationand/or drawings of Japanese Patent Application No. 2009-117972 filed onMay 14, 2009, which is a priority document of the present application.

The objects, features, advantages and ideas of the invention will beapparent to those skilled in the art from the description herein, andthose skilled in the art will be able to readily perform the invention.The best mode for carrying out the invention and specific examples, etc.which show preferred embodiments of the invention, are given by way ofillustration or explanation, and are not intended to limit the inventionthereto. It will be apparent to those skilled in the art that variousmodifications may be made based on described aspects in thespecification without departing from the spirit and scope of theinvention disclosed herein.

Sequence numbers in the Sequence Listing herein indicate the followingsequences.

SEQ ID NO: 1 shows the nucleotide sequence of DNA of CLI-ESNA. Thisnucleotide sequence shows the nucleotide sequence at positions 88 to 657in SEQ ID NO: 3 or the nucleotide sequence at positions 112 to 681 inSEQ NO; 5.

SEQ ID NO: 2 shows the amino acid sequence of CLI-ESNA. This amino acidsequence shows the amino acid sequence at positions 30 to 218 in SEQ IDNO; 4 or the amino acid sequence at positions 38 to 226 in SEQ ID NO: 6.

SEQ ID NO: 3 shows the nucleotide sequence of DNA encoding the proteinbearing CLI-ESNA, which was inserted into the expression vectorBlu-CLI-ESNA constructed in EXAMPLE 1.

SEQ ID NO: 4 shows the amino acid sequence of the protein bearingCLI-ESNA encoded by the expression vector pBlu-CLI-ESNA constructed inEXAMPLE 1.

SEQ ID NO: 5 shows the nucleotide sequence of DNA encoding the proteinbearing CLI-ESNA, which was inserted into the expression vectorpiP-H-CLI-ESNA constructed in EXAMPLE 3.

SEQ ID NO: 6 shows the amino acid sequence of the protein bearingCLI-ESNA, which is expressed by the expression vector piP-H-CLI-ESNAconstructed in EXAMPLE 3.

SEQ ID NO: 7 shows the nucleotide sequence of primer CLI-1N/Xbal used inEXAMPLE 1.

SEQ ID NO: 8 shows the nucleotide sequence of primer CL-I_S140P-R usedin EXAMPLE 1.

SEQ ID NO: 9 shows the nucleotide sequence of primer CL-I_S140P-F usedin EXAMPLE 1.

SEQ ID NO: 10 shows the nucleotide sequence of primer CLI-2-C/SalI usedin EXAMPLE 1.

SEQ ID NO; 11 shows the nucleotide sequence of primer CL-I_E110D-R usedin EXAMPLE 1.

SEQ ID NO: 12 shows the nucleotide sequence of primer CL-I_E110D-F usedin EXAMPLE 1.

SEQ ID NO: 13 shows the nucleotide sequence of primerCL*28_N179T,A180S-R used in EXAMPLE 1.

SEQ ID NO: 14 shows the nucleotide sequence of primer CLI-N-EL-SacI usedin EXAMPLE 3.

SEQ ID NO: 15 shows the nucleotide sequence of primer CLI-C-XboI used inEXAMPLE 3.

SEQ ID NO; 16 shows the nucleotide sequence of cDNA clone ph41 of CLI.

SEQ ID NO: 17 shows the amino acid sequence deduced from the nucleotidesequence of cDNA clone ph41 of CLI.

SEQ ID NO: 18 shows the nucleotide sequence of CLI. This nucleotidesequence shows the nucleotide sequence at positions 28 to 597 in SEQ IDNO: 16.

SEQ ID NO: 19 shows the amino acid sequence of CU. This amino acidsequence shows the amino acid sequence at positions 10 to 198 in SEQ IDNO: 17.

Hereinafter., the present invention is described by referring toEXAMPLES but is not deemed to be limited thereto.

EXAMPLE 1

Construction of Recombinant Apoclytin Gene

The apoclytin gene fragmemt was obtained by PCR using apoclytin geneencoding apoclytin as a template, and was inserted into a expressionvector pBlueScript SK(+) (Stratagem) and the luminescence patterns wereanalyzed.

Specifically, pBlue-CLI-ESNA was constructed by the followingprocedures.

PCR was carried out using a PCR kit (manufactured by Takara Bio) withpPh41(described in FEBS Lett. 315 (1993) 343-346) as a template and twoPCR primers of CLI-1N/XbaI (5′ c ggT CTA GAA GTC AAA CTC AGA CCC AAC TTC3′ (SEQ ID NO: 7)) and CL-I_S140P-R(5′ GTC TGA TGG GCA GAT TCC AGA 3′(SEQ ID NO: 8)) (cycle conditions: with 25 cycles of 1 min./94° C., 1min/50° C. and 1 min./72° C.). In a similar manner, PCR was performedusing the PCR kit with pPH41 as a template and two PCR primers ofCL-I_S140P-F (5′ ATC TGC CCA TCA GAC GAA GAC 3′ (SEQ ID NO: 9)) andCLI-2-C/SalI (5′ ggc GTC GAC TTA AGO AAC AAA ATT GCC OTA 3 (SEQ ID NO:10)). PCR was performed using the PCR kit with the resulting each DNAfragment as a template and two PCR primers of CLI-1N/XbaI andCLI-2-C/SalI to amplify the desired apoclytin gene region. The resultingDNA fragment was purified using a PCR purification kit (manufactured byQiagen). The purified DNA fragment was then digested with restrictionenzymes XbaI/SalI in a conventional manner, and ligated into therestriction enzyme XbaI/SalI sites on pBlueScriptSK(+) (Stratagene),thereby to construct the expression vector pBlue-CL-S140P. Thenucleotide sequence was determined using a DNA sequencer (manufacturedby ABI) to confirm the insert DNA.

Next, PCR was performed using a PCR kit with pBlue-CL-S140P as atemplate and two PCR primers of CLI-1N/XbaI and CL-I_E110D-R (5′ AAC AGCATC TCC CCA GTC GCG 3′ (SEQ ID NO: 11)). PCR was performed using the PCRkit similarly with pBlue-CL-S140P as the template and two PCR primers ofCL-I_E110D-F (5′ TOG GGA GAT GCT GTT TTC GAC 3′ (SEQ ID NO: 12)) andCL*28_N179T,A180S-R (5′ ggc GTC GAC TTA AGG AAC AAA ATT GCC GTA AAG ACCATC ACT AGT GGG 3′ (SEQ ID NO: 13)). PCR was performed using a PCR kitwith the resulting each DNA fragment as a template and the two PCRprimers of CU-1N/XbaI and CL*28_N179T,A180S-R to amplify the desiredapoclytin gene region. The resulting DNA fragment was purified using thePCR purification kit. The purified DNA fragment was then digested withrestriction enzymes XbaI/SalI in a conventional manner and ligated intothe restriction enzyme XbaI/SalI sites on pBlueScriptSK(+) (Stratagene),thereby to construct the expression vector pBlue-CLI-ESNA (FIG. 1).

The nucleotide sequence was determined using a DNA sequencer(manufactured by ABI) to confirm the insert DNA. The nucleotide sequenceof DNA encoding recombinant apoclytin-ESNA inserted into p.Blue-CLI-ESNAis shown by SEQ ID NO: 3. The amino acid sequence of the protein encodedby the polynucleotide consisting of the nucleotide sequence representedby SEQ ID NO: 3 is shown by SEQ ID NO: 4.

EXAMPLE 2

Expression of Recombinant Apoclytin in E. coli

The recombinant apoclytin gene was expressed in E. coli, using host E.coli JM83 (ATCC Accession No. 35607) bearing the vector prepared inEXAMPLE 1 wherein the recombinant apoclytin gene was inserted intopBiueScript SK(+). The transformant was inoculated onto 10 ml of LBliquid medium (10 g of bactotryptone, 5 g of yeast extract and 5 g ofsodium chloride per liter of water; pH 7.2) containing ampicillin (100μg/ml) followed by further incubation at 37° C. for 18 hours. Thecultured cells were harvested by centrifugation for 5 minutes at 10,000rpm using a cooling centrifuge, and suspended in 30 mM Tris-HCl (pH 7.6)containing 10 mM EDTA. The suspension was ultrasonicated (manufacturedby Branson, Sonifier model 250) on ice to recover the supernatant.

EXAMPLE 3

Construction of Recombinant Apoclytin-ESNA Expression Vector(piP-H-CLI-ESNA)

In order to express recombinant apoclytin-ESNA in E. coli, expressionvector piP-H-CLI-ESNA was obtained by inserting pBlue-CLI-ESNA bearingthe recombinant apoclytin-ESNA gene, which was prepared by PCR, into theexpression vector piP-H-M(11) described in EXAMPLE 4 of JPA 2008-22848.

Specifically, the recombinant apoclytin-ESNA expression vectorpiP-H-CLI-ESNA was constructed by the following procedures.

PCR was performed using a PCR kit with recombinant apoclytin-ESNAgene-bearing pBlue-CLI-ESNA as a template and two PCR primers ofCLI-N-EL-SacI (5′ ggc gAg CTC AGA CCC AAC TTC GAC AAC 3′ (SEQ ID NO:14), wherein the SacI restriction enzyme site is underlined) andCLI-C-XhoI (5′ cgg CTC GAG TTA AGG AAC AAA ATT GCC GTA 3′ (SEQ ID NO:15), wherein the XhoI restriction enzyme site is underlined) to amplifythe desired recombinant apoclytin-ESNA gene region. The resulting DNAfragment was purified using the PCR purification kit. The purified DNAfragment was then digested with restriction enzymes SacI/XhoI in aconventional manner, and ligated into the restriction enzyme SacI/XhoIsites on piP-H-M(11), thereby to construct vector piP-H-CLI-ESNA shownin FIG. 2.

The nucleotide sequence was determined using a DNA sequencer(manufactured by ABI) to confirm the insert DNA. The nucleotide sequenceof DNA encoding recombinant apoclytin-ESNA inserted into piP-H-CLI-ESNAis shown by SEQ ID NO: 5. The amino acid sequence of the protein encodedby the polynucleotide consisting of the nucleotide sequence representedby SEQ ID NO: 5 is shown by SEQ ID NO: 6.

EXAMPLE 4

Purification of Protein

1) Expression of Protein in E. coli

The expression vector piP-H-CLI-ESNA was transformed into E. coli strainWA802 (ATCC Accession No. 33526) in a conventional manner. The resultingtransformant was inoculated onto 10 ml of LB liquid medium (10 g ofbactotryptone, 5 g of yeast extract and 5 g of sodium chloride per literof water; pH 7.2) containing ampicillin (100 μg/ml) followed by furtherincubation at 37° C. for 18 hours. The cultured cells were added to 2liters of fresh LB liquid medium (400 ml×5) and cultured at 37° C. for18 hours. The cultured cells were then harvested by centrifugation for 5minutes at 5,000 rpm (6,000×g) using a cooling centrifuge.

2) Extraction of apoclytin-ESNA Protein from Cultured Cells

The cells harvested in 1) above were suspended in 200 ml (40 ml×5) of 50mM Tris-HCl (pH 7.6), and sonicated three times for 3 minutes each onice (manufactured by Branson, Sonifier model 250). The cell lysate wasthen centrifuged at 10,000 rpm (12,000×g) for 20 minutes. The resultingsoluble fraction was used as the starting material for purification ofapoclytin-ESNA protein.

3) Purification of Recombinant apoclytin-ESNA Protein by Nickel ChelateColumn Chromatography

The soluble fraction (200 ml) obtained in 2) above was applied to anickel chelate column (Amersham Bioscience; column size: 6.5 cm indiameter×2.5 cm), which had been equilibrated with 50 mM Tris-HCl (pH7.6) to adsorb the recombinant apoclytin-ESNA protein. After washingwith 200 ml of 50 mM Tris-HCl (pH 7.6), the adsorbed recombinantapoclytin-ESNA protein was eluted with 0.1M imidazole (Wako PureChemical Industries). The luminescence activity of each fraction wasassayed and the fractions having the luminescence activity werecollected.

4) Regeneration of Recombinant apoclytin-ESNA Protein into Recombinantclytin-ESNA Protein

The recombinant apoclytin-ESNA protein was regenerated to therecombinant clytin-ESNA protein under the following conditions.

The purified recombinant apoclytin-ESNA protein (20 ml) obtained in 3)above was dissolved in 80 ml of 50 mM Tris-HCl (pH 7.6) containing 10 mMDTT and 10 mM EDTA, and 0.4 mg of coelenterazine dissolved in ethanolwas added to the solution. The mixture was allowed to stand at 4° C.overnight thereby to regenrate to the recombinant clytin-ESNA protein,

5) Purification of Recombinant clytin-ESNA Protein by Butyl SepharoseColumn Chromatography

To separate the recombinant clytin-ESNA protein which formed a complexwith coelenterazine from the recombinant apoclytin-ESNA protein whichdid not form the complex, the hydrophobic chromatography using ButylSepharose 4 Fast Flow Gel was perfomed. That is, the recombinantclytin-ESNA protein (150 ml) obtained in 4) above was adjusted to 2M ina final concentration of ammonium sulfate. Next, the insoluble fractionwas removed by centrifugation. The supernatant was adsorbed to a ButylSepharose 4 Fast Flow column (Amersham Bioscience, column size, 6.0 cmin diameter×1.5 cm), which had been equilibrated with 10 mM Tris-HCl, 2mM EDTA (pH 7.6) containing 2M ammonium sulfate, and then the column waswashed with 2M ammonium sulfate. After elution with 1.2M ammoniumsulfate, the recombinant clytin-ESNA fraction having the luminescenceactivity was recovered. On the other hand, the recombinantapoclytin-ESNA was only eluted with 10 mM Tris-HCl, 2 mM EDTA (pH 7.6).

The protein concentration was determined by a commercial kit(manufactured by BioRad) by the method of Bradford, using bovine serumalbumin (manufactured by Pierce) as a standard.

SDS-PAGE analysis was performed on each fraction obtained from eachpurification step under reducing conditions using a 12% polyacrylamidegel. FIG. 3 shows the results of SDS-PAGE analysis. From 2 liters of thecultured cells, 5.3 mg of the recombinant clytin-ESNA was obtained in apurity of 95%.

EXAMPLE 5

Measurement of Luminescence Activity

The luminescence activity of the recombinant clytin-ESNA of EXAMPLE 4was measured as follows. After mixing 2-mercaptoethanol (1 μl) andsubstrate coelenterazine (1 μg/μl dissolved in ethanol) with 30 mMTris-HCl (pH 7.6) containing 10 mM EDTA, the recombinant apoclytin-ESNAat each purification step was added to the mixture. The reaction wascarried out on ice (4° C.) for 2 hours to regenerate recombinantclytin-ESNA. The luminescence reaction was triggered by adding a 50 mMcalcium solution (100 μl/well) to 1 μl of this regenerated recombinantclytin-ESNA solution. The luminescence activity was measured for 10seconds using a luminescence plate reader Centro LB960 (manufactured byBerthold) and expressed in terms of the maximum luminescence intensity(Imax).

EXAMPLE 6

Comparison of Recombinant clytin-ESNA with Other Photoproteins forLuminescence Activity

In order to compare the luminescence properties between the recombinantclytin-ESNA (CLI-ESNA) obtained in EXAMPLE 5 and other holoproteins(aequorin (AQ)), clylin-I (CL-I), clytin-II (CL-II)) and obelin (Ob)),the luminescence patterns triggered by the addition of calcium werecompared.

The luminescence patterns of CLI-ESNA, AQ, CL-I, CL-II and Ob weremeasured as follows. 2-Mercaptoethanol (1 μl) and a solution ofsubstrate coelenterazine (1 μg/μl) in ethanol were mixed with 30 mMTris-HCl (pH 7.6) containing 10 mM EDTA. Each of CLI-ESNA, AQ, CL-I,CL-II and Ob was then added to the mixture and the reaction was carriedout for 2 hours on ice (4° C.) for reconstitution, respectively. Theluminescence reaction was initiated by adding 100 μl/well of a 50 mMcalcium solution to this reconstitution solution. The luminescenceactivity was measured for 10 seconds using a luminescence plate readerCentro LB960 (manufactured by Berthold) and expressed in terms of themaximum luminescence intensity (Imax).

The results are shown in FIG. 4. As shown in FIG. 4, the luminescencepatterns were compared between the recombinant clytin and otherphotoproteins for their relative luminescence activities. Therecombinant clytin-ESNA showed a rapid decay pattern of the luminescencepatterns as compared to AQ, CI-I, Ob, etc. The results reveal that therecombinant clytin-ESNA reconstituted from the recombinantapoclytin-ESNA having 4 amino acid mutations shows a higher S/N ratiothan Cl-I.

REFERENCE EXAMPLE 1

Synthesis of Coelenteramide

4-Methoxyphenylacetyl chloride (Aldrich), 1.0M CH₂Cl₂ solution of BBr₃(Aldrich) and all other chemical reagents used in the synthesis arecommercially available and used as provided.

In thin layer chromatography (TLC) for analysis, a silica gel plateprecoated with silica gel (0.25 mm) (MERCK, Silica gel 60 F₂₅₄,Catalogue No. 1.05715.0009) was used.

For preparatory column chromatography, silica gel (Kanto Chemical,silica gel 60N, spherical, neutral, Catalogue No. 37563-84) was used.

Melting points (Mp.) were measured on YANACO MP-J3 (uncorrected), ¹H(300 MHz) nuclear magnetic resonance spectra (NMR spectra) and ¹³C (75.5MHz)

NMR spectra were measured in DMSO-d₆ (CIL) on a Varian Gemini-300. The¹H NMR chemical shifts were referenced to the peak of a residualnon-deuterated dimethylsulfoxide in a measurement solvent DMSO-d₆ set atδ 2.49 as a standard. The ¹³C NMR chemical shifts were referenced to thepeak of measurement solvent DMSO-d₆ set at δ 39.7 as a standard. Thechemical shifts are indicated by unit ppm, respectively. The bindingconstant (J) is given by unit Hz. Abbreviations s, m and hr designatesinglet, multiplet and broad, respectively. Infrared spectroscopic (IR)spectrum was measured by diffuse reflectance spectroscopy using aspectrometer SHIMADZU IRPrestige-21 equipped with DRS-8000A. Theabsorption zone was shown by unit cm⁻¹. High resolution massspectrometry (HRMS) was performed using a mass spectrometer EOL JMS-700under the conditions for electron impact ionization (EI).

Synthetic Scheme of Coelenteramide

Coelenteramide Dimethyl Ether (IV)

In an argon atmosphere, 4-(dimethylamino)pyridine (DMAP) (21.1 mg, 172μmol) and 4-methoxyphenylacetyl chloride (III) (527 μL, 3.45 mmol) weresubsequently added to a solution (5 mL) of2-amino-3-benzyl-5-(4-methoxyphenyl)pyrazine (II) (also known ascoelenteramine methyl ether) (Kishi et al., Tetrahedron Lett., 13,2747-2748 (1972); Adamczyk et al. Org. Prep. Proced. Int., 33, 477-485(2001)) (502 mg, 1.72 mmol) in pyridine at room temperature. Theresulting mixture was agitated at the same temperature for 2.5 hours.Saturated sodium hydrogencarbonate aqueous solution (100 mL) was addedto the mixture. Extraction of the mixture was performed usingdichloromethane (50 mL×3). The organic extract was dried over anhydroussodium sulfate, filtered and concentrated under reduced pressure. Theresidual pyridine was removed azeotropically with toluene (20 mL×3). Theresidue was purified by silica gel chromatography (85 g,dichloromethane/ethyl acetate=9/1) to give coelenteramide dimethyl ether(IV) (617 mg, 81.5%) as a pale yellow solid. Recrystallization fromethyl acetate cave a colorless solid as an analytically pure sample(recrystallization twice in total gave 458 mg, 60.5%),

Mp. 189.5-191° C.; ¹H NMR (300 MHz, DMSO-d₆) δ3.61 (s, 2H)3.73 (s, 3H),3.80 (s, 3H), 4.03 (s, 2H), 6.88-6.93 (AA′BB′, 2H), 7.02-7.07 (2×AA′BB′,4H), 7.12-7.30 (m, 5H), 8.00-8.05 (AA′BB′, 2H), 8.87 (s, ¹H), 10.43 (s,¹H); ¹³C NMR (75.5 MHz, DMSO-d₆) δ 41.6, 55.1, 55.3, 113.9 (2C), 114.5(2C), 126.2, 127.5, 128.0(2C), 128.1, 128.2 (2C), 129.0 (2C), 130.2(2C), 137.1, 138.3, 143.7, 148.2, 150.5, 158.2, 160.7, 170.3; IR (KBr,cm⁻¹) 698, 833, 1034, 1177, 1256, 1495, 1514, 1543, 1672, 2833, 2957,3265; HRMS (EI) m/z 439.1898 (M⁺, C₂₇H₂₅N₃O₃ requires 439.1896).

Coelenteramide (I)

In an argon atmosphere, a solution (20 mL) of coelenteramide dimethylether (IV)(660 mg, 1.50 mmol) was added to 1.0 M dichloromethanesolution of boron tribromide (6.01 mL, 6.01 mmol) at 0° C. over 10minutes. The mixture was agitated at the same temperature for 15minutes. The mixture was warmed to room temperature. The agitation wascontinued for 21 hours. Saturated sodium hydrogencarbonate (100 mL) wasadded to the mixture. The mixture was concentrated under reducedpressure to remove dichloromethane. The residual aqueous suspension wasfiltered. The solid recovered was dried in vacuum to give coelenteramide(I) (570 mg, 92.3%) as a pale yellow solid.

Recrystallization from ethanol gave a colorless solid (103 mg, 16.7%) asan analytically pure sample.

Mp. 242-243° C. (dec.); ¹H NMR (300 MHz, DMSO-d₆) δ 3.54 (s, 2H), 4.01(s, 2H), 6.69-6.75 (AA′BB′, 2H), 6.84-6.90 (AA′BB′, 2H), 7.00-7.06(AA′BB′, 2H), 7.11-7.24 (m, 5H), 7.89-7.95 (AA′BB′, 2H), 8.80 (s, ¹H),9.28 (br s, ¹H), 9.85 (br s, ¹H), 10.35 (s, ¹H); ¹³C NMR (75.5 MHz,DMSO-d₆) δ 41.7, 115.2 (2C), 115.8 (2C), 125.7, 126.2, 126.6, 128.0(2C), 128.2 (2C), 129.0 (2C), 130.2 (2C), 136.8, 138.4, 143.4, 148.6,150.5, 156.2, 159.1, 170.5; IR (KBr, cm⁻¹) 704, 1157, 1229, 1267, 1364,1450, 1493, 1516, 1545, 1593, 1611, 1673, 3022, 3285, 3385; HRMS (EI)m/z 411.1582 (M⁺, C₂₅H₂₁N₃O₃ requires 411.1583).

EXAMPLE 7

Preparation of Novel Synthetic Fluorescent Proteins from Coelenteramideand Recombinant Apoclytin-ESNA

Recombinant apoclytin-ESNA (0.5 mg, 22 nmol) (the product obtained inEXAMPLE 4, 3)) was mixed with 10 μl of coelenteramide (1.2 μg/μl inanhydrous methanol, 29 nmol)(the product obtained in REFERENCEEXAMPLE 1) in 1 ml of 50 mM Tris-HCl (pH 7.6) containing 10 mM CaCl₂ and1 mM DTT. The mixture was allowed to stand at 4° C. for 16 hours tosynthesize a fluorescent protein. Subsequently, the photoprotein wastreated at 4° C. under 5,000×g for 20 minutes using a centrifugalconcentrator Amicon Ultra-4 (10,000 MWCO, MILLIPORE) to remove an excessof coelenteramide, thereby to concentrate the mixture to 0 ml. Theconcentrated solution showed a strong yellow fluorescence under along-wavelength UV lamp (366 nm). As shown in FIG. 5, the fluorescencespectrum having the fluorescence maximum wavelength at 513 nm wasobtained by excitation at wavelength 335 nm (spectrum B in FIG. 5).

EXAMPLE 8

Preparation of Calcium-Free Novel Synthgtic Fluorescent Proteins fromCoelenteramide and Recombinant Apoclytin-ESNA

Recombinant apoclytin-ESNA (0.5 mg, 22 nmol) (the product obtained inEXAMPLE 4, 3)) was mixed with 10 μl of coeleriteramide (1.2 μg/μl inanhydrous methanol, 29 nmol)(the product obtained in REFERENCEEXAMPLE 1) in 1 ml of 50 mM Tris-HCl (pH 7.6) containing 10 mM EDTA and1 mM DTT. The mixture was allowed to stand at 4° C. for 16 hours tosynthesize a calcium-free fluorescent protein. Subsequently, thephotoprotein was treated at 4° C. under 5,000×g for 20 minutes using acentrifugal concentrator Amicon Ultra-4 (10,000 MWCO, MILLIPORE) toremove an excess of coelenteramide, thereby to concentrate the mixtureto 0.1 ml. As shown in FIG. 5, the fluorescence spectrum having thefluorescence maximum wavelength at 513 nm was obtained by excitation atwavelength 335 nm (spectrum C in FIG. 5).

EXAMPLE 9

Measurement of Fluorescence and Bioluminescence Emission Spectra

Fluorescence spectra of the synthetic fluorescent proteins in EXAMPLES 7and 8 were measured at 25° C. in a quartz cell (optical path length: 10mm) using a Jasco FP-6500 spectrofluorimeter (band width foremission/excitation: 3 nm, responses 0.5 sec, scan speed: 100 nm/min).

Bioluminescence emission spectra of the recombinant clytin-ESNA obtainedin EXAMPLE 4, 5) were measured in a quartz cell having a 10 mm opticalpath under the given conditions (band width for emission/excitation: 20nm, response: 0.5 sec, scan speed: 2000 nm/min) using a fluorescencespectrophotometer (JASCO FP-6500) with the excitation source turned off.As shown in FIG. 5, the emission spectrum having the emission maximumwavelength at 470 nm was obtained by adding 0.1 ml of 50 mM CaCl₂ to 1ml of 50 mM Tris-HCl (pH 7.6) containing the purified recombinantclytin-ESNA (0.02 mg) (spectrum A in FIG. 5).

Correction was made for the fluorescence and bioluminescence emissionspectra thus obtained.

As shown in FIG. 5, the fluorescence spectra obtained from the syntheticfluorescent proteins in EXAMPLES 7 and 8 showed the emission maximumwavelength of 513 nm, which shifted toward a longer wavelength by about43 nm or more. That is, the novel fluorescent proteins showing markedlydifferent fluorescence spectra from bioluminescence emission spectracould be prepared from apoclytin-ESNA.

The protein of the present invention can form the holoprotein composedof the protein of the present invention and the peroxide ofcoelenterazine as a luminescence substrate. The holoprotein of theinvention exists as a complex produced from the protein of the inventionand the peroxide of coelenterazine. When calcium ions are bound to thecomplex, a flash of light is emitted. This luminescence shows at leastone of the excellent properties that the decay of luminescence is rapidand the S/N ratio is excellent.

Accordingly, the protein of the invention, the holoprotein of theinvention and so on can be suitably used for the detection ormeasurement of calcium ions. Furthermore, the protein of the invention,the holoprotein of the invention, etc. can be used for the assay oftranscription activity of promoters, etc. as a reporter protein.Moreover, the holoprotein of the invention, etc. can also be used asdetection markers, materials for amusement products, and so on.

The polynucleotide of the invention encodes the protein of the inventiondescribed above, and can be used as a reporter gene.

The polynucleotide of the invention, the vector of the invention, thetransformant of the invention, etc. can be used to produce the proteinof the invention.

The invention claimed is:
 1. A polynucleotide comprising apolynucleotide encoding a protein as defined by any one of (a) through(c) below: (a) a protein consisting of the amino acid sequence of SEQ IDNO:2; (b) a protein comprising the amino acid sequence of SEQ ID NO:2,and having the binding ability to the peroxide of coelenterazine or theperoxide of a coelenterazine derivative to form a holoprotein that emitslight by calcium ions; and (c) a protein comprising a mutant of theamino acid sequence of SEQ ID NO:2, wherein one to four amino acid(s)are substituted with other amino acid(s) except for the amino acid(s) atpositions 107, 110, 120, 140, 179 and 180, and having the bindingability to the peroxide of coelenterazine or the peroxide of acoelenterazine derivative to form a holoprotein that emits light bycalcium ions.
 2. A recombinant vector comprising the polynucleotideaccording to claim
 1. 3. A transformant having inserted therein therecombinant vector according to claim
 2. 4. A method of producing aprotein, which comprises culturing a transformant having insertedtherein a recombinant vector comprising the polynucleotide of claim 1and producing the protein as defined by any one of (a) through (c).
 5. Akit comprising the polynucleotide of claim
 1. 6. A method of detectingor quantifying a calcium ion, which comprises contacting a protein asdefined by any one of (a) through (c) below: (a) a protein consisting ofthe amino acid sequence of SEQ ID NO. 2; (b) a protein comprising theamino acid sequence of SEQ ID NO: 2, and having the binding ability tothe peroxide of coelenterazine or the peroxide of a coelenterazinederivative to form a holoprotein that emits light by calcium ions; and(c) a protein comprising a mutant of the amino acid sequence of SEQ IDNO. 2, wherein one to four amino acid(s) are substituted with otheramino acid(s) except for the amino acid(s) at positions 107, 110, 120,140, 179, and 180, and having the binding ability to the peroxide ofcoelenterazine or the peroxide of a coelenterazine derivative to form aholoprotein that emits light by calcium ions, or a holoproteincomprising the protein and the peroxide of coelenterazine or theperoxide of a coelenterazine derivative, with a sample and measuring theluminescence generated to thereby detect or quantify a calcium ion.
 7. Amethod of assaying the activity of a sequence associated with promotercontrol, which comprises introducing a vector comprising thepolynucleotide of claim 1 and the sequence associated with promotercontrol into a host cell and measuring the luminescence generated by theprotein encoded by the polynucleotide to thereby assay the activity ofthe sequence associated with promoter control.
 8. A method of measuringchanges in intracellular calcium concentration, which comprises the stepof expressing the polynucleotide of claim 1 in a cell to form aphotoprotein, and measuring the luminescence generated by thephotoprotein to thereby measure changes in intracellular calciumconcentration.
 9. A method of producing a fluorescent protein, whichcomprises reacting a protein as defined by any one of (a) through (c)below: (a) a protein consisting of the amino acid sequence of SEQ ID NO.2; (b) a protein comprising the amino acid sequence of SEQ ID NO: 2, andhaving the binding ability to the peroxide of coelenterazine or theperoxide of a coelenterazine derivative to form a holoprotein that emitslight by calcium ions; and (c) a protein comprising a mutant of theamino acid sequence of SEQ ID NO. 2, wherein one to four amino acid(s)are substituted with other amino acid(s) except for the amino acid(s) atpositions 107, 110, 120, 140, 179 and 180, and having the bindingability to the peroxide of coelenterazine or the peroxide of acoelenterazine derivative to form a holoprotein that emits light bycalcium ions, with coelenteramide or an analogue thereof in the presenceor absence of a calcium ion or a divalent or trivalent ion that can besubstituted for the calcium ion.
 10. The method according to claim 9,wherein the reaction is carried out in the presence of a reducing agent.11. The method according to claim 9, wherein the reaction is carried outin the presence of a chelating agent to remove the calcium ion or thedivalent or trivalent ion that can be substituted for the calcium ion.